Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties

Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties

A synthetic route to novel benzofuran-fused phosphole derivatives 3–5 is described. These compounds showed optical and electrochemical properties that differ from their benzothiophene analog. Preliminary results show that 4 can be used as an emitter in OLEDs, illustrating the potential of these new...

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Main Authors: Chen, Hui, Delaunay, Wylliam, Li, Jing, Wang, Zuoyong, Bouit, Pierre-Antoine, Tondelier, Denis, Geffroy, Bernard, Mathey, François, Duan, Zheng, Réau, Régis, Hissler, Muriel
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Subjects:
DRNTU::Science::Chemistry::Organic chemistry
Online Access:https://hdl.handle.net/10356/99639
http://hdl.handle.net/10220/17401
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Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-99639
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spelling sg-ntu-dr.10356-996392020-03-07T12:34:48Z Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties Chen, Hui Delaunay, Wylliam Li, Jing Wang, Zuoyong Bouit, Pierre-Antoine Tondelier, Denis Geffroy, Bernard Mathey, François Duan, Zheng Réau, Régis Hissler, Muriel School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry A synthetic route to novel benzofuran-fused phosphole derivatives 3–5 is described. These compounds showed optical and electrochemical properties that differ from their benzothiophene analog. Preliminary results show that 4 can be used as an emitter in OLEDs, illustrating the potential of these new compounds for opto-electronic applications. 2013-11-07T07:51:38Z 2019-12-06T20:09:45Z 2013-11-07T07:51:38Z 2019-12-06T20:09:45Z 2013 2013 Journal Article Chen, H., Delaunay, W., Li, J., Wang, Z., Bouit, P. A., Tondelier, D., et al. (2013). Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties. Organic letters, 15(2), 330-333. https://hdl.handle.net/10356/99639 http://hdl.handle.net/10220/17401 10.1021/ol303260d en Organic letters
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science::Chemistry::Organic chemistry
spellingShingle DRNTU::Science::Chemistry::Organic chemistry
Chen, Hui
Delaunay, Wylliam
Li, Jing
Wang, Zuoyong
Bouit, Pierre-Antoine
Tondelier, Denis
Geffroy, Bernard
Mathey, François
Duan, Zheng
Réau, Régis
Hissler, Muriel
Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties
description A synthetic route to novel benzofuran-fused phosphole derivatives 3–5 is described. These compounds showed optical and electrochemical properties that differ from their benzothiophene analog. Preliminary results show that 4 can be used as an emitter in OLEDs, illustrating the potential of these new compounds for opto-electronic applications.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Chen, Hui
Delaunay, Wylliam
Li, Jing
Wang, Zuoyong
Bouit, Pierre-Antoine
Tondelier, Denis
Geffroy, Bernard
Mathey, François
Duan, Zheng
Réau, Régis
Hissler, Muriel
format Article
author Chen, Hui
Delaunay, Wylliam
Li, Jing
Wang, Zuoyong
Bouit, Pierre-Antoine
Tondelier, Denis
Geffroy, Bernard
Mathey, François
Duan, Zheng
Réau, Régis
Hissler, Muriel
author_sort Chen, Hui
title Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties
title_short Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties
title_full Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties
title_fullStr Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties
title_full_unstemmed Benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties
title_sort benzofuran-fused phosphole : synthesis, electronic, and electroluminescence properties
publishDate 2013
url https://hdl.handle.net/10356/99639
http://hdl.handle.net/10220/17401
_version_ 1681043017881878528

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